A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3581



Internal ID15548205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:25093363..25107202hg38UCSC Ensembl
Outerchr22:25489330..25503169hg19UCSC Ensembl
Outerchr22:23819330..23833169hg18UCSC Ensembl
Outerchr22:23813884..23827723hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3811874
hg1911874
hg1811874
hg1711874
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7734
SamplesNA12156
Known GenesKIAA1671, LOC100128531
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv3581
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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